Shengxiang Xiao

Curriculum Vitae

Sheng-Xiang Xiao, MD，PH.D

Professor, Department of Dermatology

The Second Affiliated Hospital,Xi'An Jiaotong University

157 Xiwu Road,Xi'An, Shaanxi 710004

P. R. China

Email: xiao_sx@163.com

General Information

Born in July,1962; Male;

Education

Sep.1979-July,1984 Xi'An Medical University Bachelor of Medicine

Sep.1987-Dec.1990 Xi'An Medical University Master of Medicine

May,2003-Nov.2005 Xi’an Jiaotong University PH.D

Experience

2008-present Professor, Department of Dermatology

2004-2008 Associate professor, Department of Dermatology

The Second Hospital,Xi'An Jiaotong University

1996-2004 Lecturer, Department of Dermatology

The Second Hospital,Xi'An Jiaotong University

Jan.1993-July,1995 Postgraduate Researcher, Molecular Pathology laboratory,

University of California, San Francisco

Professional Organization

2008-2018 Standing committee member, Chinese Dermatologist Association

2018-present Standing committee member,Chinese Society of dermatology

Publication

1.Xiao SX, Feng YG, Ren XR, Tan SS, Li L, Wang JM, Shi YZ.A novel mutation in the second half of the keratin 17 1A domain in a large pedigree with delayed-onset pachyonychia congenita type 2. J Invest Dermatol. 122(4):892-895,2004.(影响因子7.216)

2.Feng YG, Xiao SX, Ren XR, Wang WQ, Liu A, Pan M.Keratin 17 mutation in pachyonychia congenita type 2 with early onset sebaceous cysts.Br J Dermatol. 148(3):452-455，2003.(影响因子4.275)

3.Liu Y,Xiao SX,Peng ZH,Lei XB , Wang JM, Li Y,Li XL. Two frameshift mutations of the double-stranded RNA-specific adenosine deaminase gene in Chinese pedigrees with dyschromatosis symmetrica hereditaria. Br J Dermatol, 155(2):436-7, 2006. (影响因子4.275)

4.Zhong SY, Dong YY, Liu DX, Xu DH, Xiao SX, Chen HL, Kong MG.Surface air plasma-induced cell death and cytokine release of human keratinocytes in the context of psoriasis.Br J Dermatol. 2016 Mar;174(3):542-52(影响因子4.275)

5.Liu Y, Peng ZH, Xiao SX, Wang, JM ,Geng, SM , Zhou, X , Li, XL ,Pan, M , Lei, XB . A novel mutation of the keratin 1 gene in a family with epidermolytic hyperkeratosis.J Dermatol Sci, 43(2): 143-145. 2006. (影响因子3.419)

6.Zhou SN,Xiao SX, Peng ZH, Li BX, Li XL, Liu Y, Luo SJ.A novel mutation of the FECH gene in a Chinese family with erythropoietic protoporphyria. J Dermatol Sci, 48,145-7, 2007. (影响因子3.419)

7.Wang, XP; Wang, WJ; Wang, JM, ,Liu, Y,Xiao, SX.Four novel and two recurrent mutations of the ADAR1 gene in Chinese patients with dyschromatosis symmetrica hereditaria. J DERMATOL SCI, 58(3): 217-218, 2010. (影响因子3.419)

8.Li XL, Geng SM, Lei XB, Xiao SX, Liu Y, Peng ZH.Unusual psoriasiform lesions in a patient with Hyper-IgE syndrome.J Eur Acad Dermatol Venereol. 21(3):424-426,2007. (影响因子3.029)

9.Li XL,Xiao SX,Peng ZH,Pan, M ,Zhou, SN .A mutation in exon 1 of keratin 14 resulting in a Chinese family with epidermolysis bullosa simplex Dowling–Meara. J Eur Acad Dermatol Venereol. 21:977-914,2007. (影响因子3.029)

10.Li XL, Peng ZH, Xiao SX. A novel deletion mutation of the ATP2C1 gene in Chinese patients with Hailey-Hailey disease J Eur Acad Dermatol Venereol.2008, 22 (2 ) 253-254 (影响因子3.029)

11.Wang, XP,Huo J, Liu Y, Wang WJ, Xu QQ, Ma JH, An JG, Wang JM, Xiao SX.Chinese family with lipoid proteinosis resulting from a homozygous missense mutation in the extracellular matrix protein 1 gene . J Eur Acad Dermatol Venereol, 2009: 11; 1336-1338. (影响因子3.029)

12.Wu JW, Xiao SX. A recurrent keratin 14 mutation in Dowling-Meara epidermolysis bullosa simplex in a Chinese family. J Eur Acad Dermatol Venereol, 23(4): 484-486, 2009. (影响因子3.029)

13.Wu JW, Xiao SX, Liu Y, Yu B, Bai ZL, Zhou SN, Li XL. Identification of two recurrent mutations in keratin genes in three cases with pachyonychia congenital. J Eur Acad Dermatol Venereol, 23(2): 174-176,2009. (影响因子3.029)

14.An JG, Xiao SX, Xiao SB.Quality of life of patients with scabies.J Eur Acad Dermatol Venereol. 2010 ;24(10):1187-91. (影响因子3.029)

15.An, JG; Ma, JH; Xiao, SX, Xiao, SB , Yang, F . Quality of life in patients with lepromatous leprosy in China. J Eur Acad Dermatol Venereol: 24 (7 ): 827-832,2010. (影响因子3.029)

16.Ma J, Xiao S, An J, Wang X, Xu Q, Dong Y, Feng Y, Wang J.A novel splicing mutation and haplotype analysis of the FECH gene in a Chinese family with erythropoietic protoporphyria.J Eur Acad Dermatol Venereol. 24(6):726-729. 2010. (影响因子3.029)